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Journal of Medical Genetics|April 1, 1982
A family study of Charcot-Marie-Tooth diseaseA P Brooks, A E EmeryJournal of the Neurological Sciences|April 1, 1975
Changes in creatine kinase and its isoenzymes in human fetal muscle during developmentC D Foxall, A E EmeryJournal of Neurology, Neurosurgery, and Psychiatry|December 1, 1972
Myotonic dystrophy: investigation of the proposed defect in guanidoacetic acid synthesisC E Bolton, A E EmeryJournal of Medical Genetics|October 1, 1978
Estimation of proportion of new mutants among cases of Duchenne muscular dystrophyA M Davie, A E EmerySouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|September 24, 1983
Gaucher's disease in the black population of South Africa. A case reportP Jacobs, R Tribe, E M Petersen, et al.The Journal of Clinical Pediatric Dentistry|February 19, 2004
Crouzonodermoskeletal syndromeA Jeftha, L Stephen, J A Morkel, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|December 15, 1984
A clinical and ultrastructural study of osteogenesis imperfecta after flavonoid (Catergen) therapyC J Jones, C Cummings, J Ball, et al.American Journal of Medical Genetics|November 1, 1993
Genetic skeletal dysplasias in the Museum of Pathological Anatomy, ViennaP Beighton, E Sujansky, B Patzak, et al.International Dental Journal|September 26, 2001
Dental and oral manifestations of sclerosteosisL X Stephen, H Hamersma, J Gardner, et al.Human Genetics|July 1, 1997
Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african familiesR S Ramesar, S Bardien, P Beighton, et al.Pageof 28